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Silver-Catalyzed Diastereo- and Enantioselective Michael Addition and 1,3-Dipolar Cycloaddition Reactions of Imino Esters to 3-Methyl-4-nitro-5-styrylisoxazoles
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Citations
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References
2018
Year
EngineeringOrganic ChemistryChemistrySilver-catalyzed Diastereo-Stereoselective Synthesis1,3-Dipolar Cycloaddition ReactionsImino EstersCorresponding Michael AdductsBiochemistryCatalysisPharmaceutical ActivitiesPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringGlycine Imino EstersNatural SciencesSynthetic ChemistryDrug Discovery
The AgOAc/ThioClickFerrophos complex catalyzed conjugate additions and 1,3-dipolar cycloadditions of 3-methyl-4-nitro-5-styrylisoxazoles with 1-pyrroline-5-carboxylates and glycine imino esters to give the corresponding Michael adducts and cycloadducts, respectively, in good yields with excellent diastereo- and enantioselectivities. These reactions can provide pyrroline- or pyrrolidine-containing isoxazole hybrid molecules that have potential biological and pharmaceutical activities.
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